Prevalence of the immune evasion gene cluster in Staphylococcus aureus CC398

Christiane Cuny1, Mohamed Abdelbary1, Franziska Layer1

  • 1Robert Koch Institute, Wernigerode Branch, Burgstrasse 37, 38855 Wernigerode, Germany.

Insights

The immune evasion gene cluster (IEC) is typically found in human Staphylococcus aureus but often lost in animal strains. This study found IEC in some horse infections and veterinarians, suggesting potential readaptation in livestock-associated MRSA CC398.

Area of Science:

  • Microbiology
  • Genetics
  • Epidemiology

Background:

  • The immune evasion gene cluster (IEC) is characteristic of human Staphylococcus aureus strains.
  • Livestock-associated methicillin-resistant S. aureus (LA-MRSA) CC398, often derived from human-adapted ancestors, typically lacks the IEC.
  • Understanding IEC presence in animal-associated and human-infecting S. aureus is crucial for tracking strain evolution and host adaptation.

Purpose of the Study:

  • To investigate the prevalence of the IEC in MRSA CC398 isolates from pigs, horses, and humans with occupational animal contact.
  • To compare IEC presence in MRSA CC398 with methicillin-susceptible S. aureus (MSSA) CC398 isolates from human infections.
  • To assess the implications of IEC acquisition and loss in the context of S. aureus host adaptation and evolution.

Main Methods:

  • Collection and characterization of S. aureus isolates from various sources: pig nasal colonization, horse infections, human nasal colonization (pig farmers), veterinarian infections, and human infections.
  • Detection of the immune evasion gene cluster (IEC) using molecular methods.
  • Identification of specific Staphylococcus aureus CC398 subpopulations using PCR for canonical single nucleotide polymorphisms (SNPs) and detection of luk-PV.
  • Comparative analysis of IEC presence across different host origins and S. aureus subtypes (MRSA vs. MSSA).

Main Results:

  • The IEC was absent in pig nasal isolates but detected in some horse infections and veterinarians.
  • MRSA CC398 isolates from pig farmers were negative for IEC, while some veterinarians had positive isolates.
  • Among human MRSA CC398 infections, 19% carried the IEC, with a subset linked to the ancestral human-adapted subpopulation.
  • A significant proportion of LA-MRSA CC398 from human infections had re-acquired the IEC, not always linked to luk-PV presence.
  • MSSA CC398 isolates from human infections frequently contained the IEC, with some linked to the animal-associated subpopulation.

Conclusions:

  • The presence of the IEC in animal-associated S. aureus and its re-acquisition by LA-MRSA CC398 suggests potential readaptation to the human host.
  • IEC acquisition is not essential for LA-MRSA CC398 to cause infections in humans.
  • Distinguishing between the ancestral human-adapted and animal-associated subpopulations of CC398 is critical for accurate epidemiological surveillance.

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